ChemicalBook CAS DataBase List L-(-)-SORBOSE

L-(-)-SORBOSE synthesis

12synthesis methods

Product Name:L-(-)-SORBOSE
CAS Number:87-79-6
Molecular formula:C6H12O6
Molecular Weight:180.16

50-99-7 Synthesis

50-99-7
1001 suppliers
$6.00/25g

57-48-7 Synthesis

57-48-7
559 suppliers
$12.00/250G

87-79-6
262 suppliers
$34.00/10g

Yield:-

Reaction Conditions:

with silica zeolite beta containing Lewis acidic framework Ti⁴⁺ in methanol at 99.84; for 2 h;Kinetics;Sealed tube;Reagent/catalyst;

Steps:

2.2 Kinetic Studies of Glucose Reactions with Ti-Beta
Reactions with D-glucose (Sigma-Aldrich, ≧99%) were conducted in 10 mL thick-walled glass batch reactors (VWR), with temperature control via an oil bath located on a digital stirring hotplate (Fisher Scientific). Typical reactions with D-glucose were carried out at a 1:50 metal:glucose molar ratio and involved contacting 4 g of a 1% (w/w) glucose solution in water or in methanol with the catalytic solids in a stirred glass reactor sealed with a crimp top (PTFE/silicone septum, Agilent). Kinetic studies using isotopically-labeled glucose were performed using 1% (w/w) solutions of D-glucose-D2 (Cambridge Isotope Laboratories, ≧98%) or of D-glucose-D₂-1,2,3,4,5,6,6 (Cambridge Isotope Laboratories, ≧98%) in methanol. [0080] Reactors were placed in the oil bath and small aliquots (50-100 microliters) were extracted at various time intervals via syringe (Hamilton), filtered through a 0.2 micron PTFE filter (National Scientific), and mixed with 1% (w/w) aqueous D-mannitol (Sigma-Aldrich, ≧98%) solutions used as an internal standard for quantification. The composition of reaction aliquots was determined after separation of compounds in an Agilent 1200 high performance liquid chromatograph (HPLC) equipped with an evaporative light scattering (ELS) detector (Agilent 380 LC). Glucose, sorbose, mannose, fructose, and mannitol fractions were separated using a Hi-Plex Ca column (7.7×300 mm, 8 micron particle size, Agilent) held at 353 K, with either ultrapure water (0.010 mL s^-1flow rate) or a 30/70 (v/v) mixture of acetonitrile/water (0.013 mL s^-1flow rate) as the mobile phase.

References:

CALIFORNIA INSTITUTE OF TECHNOLOGY;DAVIS, MARK E.;GOUNDER, RAJAMANI US2014/309415, 2014, A1 Location in patent:Paragraph 0079; 0080

57-48-7 Synthesis

57-48-7
559 suppliers
$12.00/250G

849585-22-4 Synthesis